Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:21526379-21526568 | Common:1; Rare:61 | ||||
chr10:21533943-21534341 | Common:3; Rare:166 | ||||
chr10:22321357-22321512 | Rare:55 | ||||
chr10:24208769-24209184 | Common:1; Rare:117 | ||||
chr10:24238815-24239229 | Common:2; Rare:50 | ||||
chr10:24239296-24239479 | Rare:35 | ||||
chr10:24466408-24466650 | Rare:38 | ||||
chr10:24952573-24952894 | Common:3; Rare:96 | ||||
chr10:27154310-27154480 | Rare:45 | ||||
chr10:27155184-27155371 | Common:3; Rare:64; Clinvar:4; Clinvar (benign):3 | ||||
chr10:27240478-27240628 | Common:1; Rare:48 | ||||
chr10:27240715-27240889 | Rare:48 | ||||
chr10:27242058-27242235 | Common:1; Rare:76 | ||||
chr10:28532631-28532819 | Common:1; Rare:79 | ||||
chr10:28533002-28533227 | Rare:91 |